Evidence map›Paper›PMID 28818100›Full record

ArticleMolecular cancer2017

miR-140-5p suppresses the proliferation, migration and invasion of gastric cancer by regulating YES1.

Zheng Fang, Shuai Yin, Ruochuan Sun, Shangxin Zhang, Min Fu, Youliang Wu, Tao Zhang, Junaid Khaliq, Yongxiang Li

Open access · goldAbstract read
In one paragraph

Article in Molecular cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 2 pooled it
7.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

87 citing papers in PubMed, 2 syntheses or guidelines pooled it, 148 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  11. Salivary Extracellular Vesicles: Biomarkers and Beyond in Human Diseases.International journal of molecular sciences · 2023
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  16. MicroRNA in adenoid cystic carcinoma (Review).International journal of oncology · 2023
    Review
  17. Article
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  20. Article

27 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Zheng FangDepartment of General Surgery, First affiliated Hospital of Anhui Medical University, 218 Jixi Avenue, Hefei, 230022, China.
Shuai YinDepartment of General, Visceral, Transplantation, Vascular and Thoracic Surgery, Hospital of University of Munich, Marchioninistr.15, 5H-02-428, 81377, Munich, Germany.
Ruochuan SunDepartment of General Surgery, First affiliated Hospital of Anhui Medical University, 218 Jixi Avenue, Hefei, 230022, China.
Shangxin ZhangDepartment of General Surgery, First affiliated Hospital of Anhui Medical University, 218 Jixi Avenue, Hefei, 230022, China.
Min FuDepartment of General Surgery, First affiliated Hospital of Anhui Medical University, 218 Jixi Avenue, Hefei, 230022, China.
Youliang WuDepartment of General Surgery, First affiliated Hospital of Anhui Medical University, 218 Jixi Avenue, Hefei, 230022, China.
Tao ZhangDepartment of General Surgery, First affiliated Hospital of Anhui Medical University, 218 Jixi Avenue, Hefei, 230022, China.
Junaid KhaliqDepartment of General Surgery, First affiliated Hospital of Anhui Medical University, 218 Jixi Avenue, Hefei, 230022, China.
Yongxiang LiDepartment of General Surgery, First affiliated Hospital of Anhui Medical University, 218 Jixi Avenue, Hefei, 230022, China. yongxiangli_1@hotmail.com.
Anhui Medical University · CNFirst Affiliated Hospital of Anhui Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aberrant expression of microRNA-140-5p (miR-140-5p) has been described in gastric cancer (GC). However, the role of miR-140-5p in GC remains unclear. In this study, the prognostic relevance of miR-140-5p in GC was investigated and YES1 was identified as a novel target of miR-140-5p in regulating tumor progression.

methodsmiR-140-5p level was determined in 20 paired frozen specimens through quantitative real-time PCR, and analyzed in tissue microarrays through in situ hybridization. The target of miR-140-5p was verified through a dual luciferase reporter assay, and the effects of miR-140-5p on phenotypic changes in GC cells were investigated in vitro and in vivo.

resultsCompared with that in adjacent normal tissues, miR-140-5p expression decreased in cancerous tissues. The downregulated miR-140-5p in 144 patients with GC was significantly correlated with the reduced overall survival of these patients. miR-140-5p could inhibit GC cell proliferation, migration and invasion by directly targeting 3'-untranlated region of YES1. miR-140-5p could also remarkably reduce the tumor size in GC xenograft mice.

conclusionsmiR-140-5p serves as a potential prognostic factor in patients with GC, and miR-140-5p mediated YES1 inhibition is a novel mechanism behind the suppressive effects of miR-140-5p in GC.

Indexed as

MicroRNAsAnimalsCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticHumansImmunohistochemistryMiceMice, Inbred BALB CNeoplasm InvasivenessPrognosisProto-Oncogene Proteins c-yesStomach NeoplasmsXenograft Model Antitumor AssaysMicroRNAsMirn140 microRNA, humanProto-Oncogene Proteins c-yesYES1 protein, humangastric cancermiR-140-5pprognostic factortumor progressionYES1

Identifiers

PMID28818100
PMCPMC5561618
OpenAlexW2746324226

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.